Human and mouse trigeminal ganglia cell atlas implicates multiple cell types in migraine.
Human and mouse trigeminal ganglia cell atlas implicates multiple cell types in migraine.
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DOI:
10.1016/j.neuron.2022.03.003
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发表时间:
2022-06-01
期刊:
影响因子:
16.2
通讯作者:
Renthal, William
中科院分区:
文献类型:
--
作者:
Yang, Lite;Xu, Mengyi;Bhuiyan, Shamsuddin A.;Li, Jia;Zhao, Jun;Cohrs, Randall J.;Susterich, Justin T.;Signorelli, Sylvia;Green, Ursula;Stone, James R.;Levy, Dan;Lennerz, Jochen K.;Renthal, William
Sensitization of trigeminal ganglion neurons contributes to primary headache disorders such as migraine, but the specific neuronal and non-neuronal trigeminal subtypes that are involved remain unclear. We thus developed a cell atlas in which human and mouse trigeminal ganglia are transcriptionally and epigenomically profiled at single-cell resolution. These data describe evolutionarily conserved and human-specific gene expression patterns within each trigeminal ganglion cell type, as well as the transcription factors and gene regulatory elements that contribute to cell-type-specific gene expression. We then leveraged these data to identify trigeminal ganglion cell types that are implicated both by human genetic variation associated with migraine and two mouse models of headache. This trigeminal ganglion cell atlas improves our understanding of the cell types, genes, and epigenomic features involved in headache pathophysiology and establishes a rich resource of cell-type-specific molecular features to guide the development of more selective treatments for headache and facial pain. Trigeminal ganglion neurons are activated in migraine and related headache disorders. Yang et al. developed a cell atlas in which human and mouse trigeminal ganglia are transcriptionally and epigenomically profiled at single-cell resolution. These data provide a rich resource for understanding the cell types and genetic mechanisms underlying migraine susceptibility and for developing novel analgesics.
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影响因子:
30.8
作者:
Fulco, Charles P.;Nasser, Joseph;Engreitz, Jesse M.
通讯作者:
Engreitz, Jesse M.
影响因子:
30.8
作者:
Gormley, Padhraig;Anttila, Verneri;Palotie, Aarno
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Palotie, Aarno
影响因子:
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作者:
Buenrostro JD;Wu B;Litzenburger UM;Ruff D;Gonzales ML;Snyder MP;Chang HY;Greenleaf WJ
通讯作者:
Greenleaf WJ
影响因子:
11.2
作者:
DeFelice, Milena;Eyde, Nathan;Dodick, David;Dussor, Gregory O.;Ossipov, Michael H.;Fields, Howard L.;Porreca, Frank
通讯作者:
Porreca, Frank
DOI:
10.1126/science.abf9277
发表时间:
2021-07-23
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Brioschi S;Wang WL;Peng V;Wang M;Shchukina I;Greenberg ZJ;Bando JK;Jaeger N;Czepielewski RS;Swain A;Mogilenko DA;Beatty WL;Bayguinov P;Fitzpatrick JAJ;Schuettpelz LG;Fronick CC;Smirnov I;Kipnis J;Shapiro VS;Wu GF;Gilfillan S;Cella M;Artyomov MN;Kleinstein SH;Colonna M
通讯作者:
Colonna M